88-32-4
88-32-4
Chemical Structure
3-tert-Butyl-4-methoxyphenol
- CAS No.: 88-32-4
- Formula:C11H16O2
- Molecular Weight:180.24
IUPAC Name: 3-(tert-butyl)-4-methoxyphenol
InChIKey: IMOYOUMVYICGCA-UHFFFAOYSA-N
SMILES: OC1=CC=C(C(C(C)(C)C)=C1)OC
Biological Activity: 3-tert-Butyl-4-methoxyphenol is a PROTAC linker, belongs to alkyl/ether class, with insecticidal activity. 3-tert-Butyl-4-methoxyphenol also induced increased activities of glutathione (GSH) S-transferase and epoxide hydrolase in the liver and forestomach tissues of A/HeJ mice, regulating the carcinogen metabolism system[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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3-tert-Butyl-4-methoxyphenol | 99.45% | 3-tert-Butyl-4-methoxyphenol is a PROTAC linker, belongs to alkyl/ether class, with insecticidal activity. 3-tert-Butyl-4-methoxyphenol also induced increased activities of glutathione (GSH) S-transferase and epoxide hydrolase in the liver and forestomach tissues of A/HeJ mice, regulating the carcinogen metabolism system. | ||||||||||||||||||||
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3-tert-Butyl-4-methoxyphenol (Standard) | ≥98% | 3-tert-Butyl-4-methoxyphenol (Standard) is the analytical standard of 3-tert-Butyl-4-methoxyphenol. This product is intended for research and analytical applications. 3-tert-Butyl-4-methoxyphenol is a PROTAC linker, belongs to alkyl/ether class, with insecticidal activity. 3-tert-Butyl-4-methoxyphenol also induced increased activities of glutathione (GSH) S-transferase and epoxide hydrolase in the liver and forestomach tissues of A/HeJ mice, regulating the carcinogen metabolism system. | ||||||||||||||||||||
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References
- [1]. Lam LK, et al. Effects of 2- and 3-tert-butyl-4-hydroxyanisole on glutathione S-transferase and epoxide hydrolase activities and sulfhydryl levels in liver and forestomach of mice. Cancer Res. 1981 Oct;41(10):3940-3. [Content Brief]
- [2]. Insecticide for vermin of order coleoptera. Japan, JP55136202 A 1980-10-23.
